Clinical Trial Assistant, HYBRID in Wilmington, DE
IQVIA · Wilmington, DE
Clinical OperationsFull-time$36k–$123kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical trial support role assisting with documentation, regulatory compliance, and clinical operations at a global clinical research organization. Hybrid position in Wilmington, DE involving file management, case report form tracking, and potential site visit support.
What they're looking for
- Bachelor's degree
- 3 years administrative support experience
- Proficiency with Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Time management and organizational abilities
- Knowledge of GCP and ICH guidelines (company-provided training)
- Understanding of clinical protocol requirements (company-provided training)
What you'll be doing
- Update and maintain clinical documents and Trial Master File systems for compliance tracking
- Prepare, handle, distribute, and archive clinical documentation following standard procedures
- Track and manage Case Report Forms, queries, and clinical data flow
- Assist with handling and distribution of clinical trial supplies and tracking information
- Serve as central communication contact for project correspondence and documentation
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.